dc.contributorMostardeiro, Marco Aurelio
dc.contributorhttp://lattes.cnpq.br/6195396264565980
dc.contributorDalcol, Ionara Irion
dc.contributorhttp://lattes.cnpq.br/9769548819312192
dc.contributorIlha, Vinicius
dc.contributorhttp://lattes.cnpq.br/3882671719676564
dc.creatorReis, Frederico Luiz
dc.date.accessioned2018-11-27T10:41:03Z
dc.date.accessioned2019-05-24T20:31:13Z
dc.date.available2018-11-27T10:41:03Z
dc.date.available2019-05-24T20:31:13Z
dc.date.created2018-11-27T10:41:03Z
dc.date.issued2018-07-17
dc.identifierhttp://repositorio.ufsm.br/handle/1/14945
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/2841673
dc.description.abstractThe phytochemical investigation of hexane and methanolic crude extracts and their fractions from the bark of the stem of Tabernaemontana catharinensis (Apocynaceae, commonly known as cobrina) led to the isolation of nine monoterpene indole alkaloids, voachalotin, affinisine, 16-epiaffinisin, voacangin, voacristin, vinpocetine, voacangine hydroxylindolenine, 12-methoxy-N4-methyl voachalotine and 12-methoxy-N4-methyl-5-epiquachalotine. The alkaloid vinpocetine and 12- methoxy-N4-methyl-5-epi voachalotin are isolated for the first time in the family Apocynaceae. A Nmethyl affinisine derivative was obtained through an affinisin methylation reaction. The extracts, fractions and isolated compounds showed antibacterial activity (Gram-positive and Gram-negative) and effective antifungal, against the tested strains. The inhibitory potential of the pairs of diastereoisomers, corinantean skeleton, affinisine, 16-epiaffinisina and 12-methoxy-N4-methyl-5- epivoachalotine, 12-methoxy-N4-methyl voachalotine presented MIC values (1.56 μg.mL -1) lower than the fluconazole standard (MIC 3.12 μg.mL-1) compared to fungal strains. The methylation of the affinisine compound potentiated the inhibition against some microorganisms. The ibogan skeletal alkaloids, Voacangina, and Voacristina presented better inhibitory potentials against bacteria, presenting MIC of 3.12; 12.5 and 25 μg.mL -1 against the microorganisms Pseudomonas aeroginosa, Bacillus cereus and Salmonella typhimurium, respectively, being equal to or close to the chloramphenicol standard. The importance of stereochemistry in relation to the effectiveness of the MIC, which is visible in the activities presented in this paper. Thus, the phytochemical study and the pharmacological activities of the identified compounds of the stem bark of T.catharinensis broaden the knowledge alluding to chemotaxonomy, as well as justifying its antifungal use in folk medicine.
dc.publisherUniversidade Federal de Santa Maria
dc.publisherBrasil
dc.publisherQuímica
dc.publisherUFSM
dc.publisherPrograma de Pós-Graduação em Química
dc.publisherCentro de Ciências Naturais e Exatas
dc.rightshttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.subjectTabernaemontana catharinensis
dc.subjectAlcaloide indólico
dc.subjectVinpocetina
dc.subjectAtividade antimicrobiana
dc.subjectIndole alkaloid
dc.subjectVinpocetine
dc.subjectAntimicrobian activity
dc.titleInvestigação de metabólitos secundários de Tabernaemontana catharinensis A. DC. – (Apocynaceae) e suas potenciais atividades antimicrobianas
dc.typeTesis


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